Anyone know a DR in UK?

Does anyone know a good doctor in the UK?  Diagnosed via blood tests in Germany but can't get appointment re treatment until December 2011 and can't really afford to travel there for consulation and treatment!  Ideally if anyone knows a doctor in the North of England who has some awareness of the illness and treatments that would be great!

Welcome Dan

Please watch your private messages.  I think someone from the UK will be along to help.

Rica

3/9 Symptoms returning. Began 5 abx protocol 5/9 Rifampin 600, Amox 1000, Doxy 200, MWF Azith 250, flagyl 1000 daily. Began Sept 04 PPMS EDSS 6.7 Now good days EDSS 1 Mind, like parachute, work only when open. Charlie Chan  In for the duration.&am

Alternatively the Breakspear in Hertfordshire do know about stealth pathogens and will treat you.  I saw Dr M.

Good Luck

Bertie

ME/CFS, adrenal insufficiency low dose steroids + flurdrocortisone, thyroid disease Armoujr + 25 mcg T3, 25 mcg T4, 20mg Propoananol, 200 Doxy from 1/4/11, Azithro MWF from 1/6/11, Metro 1st 5 day pulse 13/7/11

Desperate Dan, you don’t say what is wrong with you.  Cpn is a pathogen, not an illness.................Sarah

A  Journey through Light and Shadow

 

Completed Stratton/Wheldon regime for aggressive secondary progressive MS in June 2007, after four years, three of which intermittent.   Still improving bit by bit and no relapses since finishing treatment.

Was diagnosed in mid 2009 with Lyme disease following a tick bite in Aug 2008 (at that time I knew nothing about Lyme disease or ticks).  Was treated with mixed anti-biotics until Feb 2011.  Symptoms were issues with pain in knees and hands, rashes & skin peeling on feet, raynaud's in hands, difficulty dealing with loud noises - all of which are alot better than they were - but main issues still remaining are nausea (often but less severe than previously) and heavy/thick/throbbing head (constantly).    Recent blood tests showed the Lyme infection had improved a great deal but now tests showed activity against Chlamydia pneumoniae and Ehrlichia

Well, the main person at present able to treat you is Sarah Myhill from Knighton, Powys, right on the Anglo Welsh border: http://www.drmyhill.co.uk/ .................Sarah

A  Journey through Light and Shadow

 

Completed Stratton/Wheldon regime for aggressive secondary progressive MS in June 2007, after four years, three of which intermittent.   Still improving bit by bit and no relapses since finishing treatment.